Canonical Allele Identifier: CA113752028

Gene: LINC02145

Linked Data

• dbSNP Id: rs975936057
• MyVariant Identifiers: chr5:g.6324239T>A (hg19) ; chr5:g.6324126T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6324126T>A , CM000667.2:g.6324126T>A	GRCh38
NC_000005.9:g.6324239T>A , CM000667.1:g.6324239T>A	GRCh37
NC_000005.8:g.6377239T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_028351.1:n.144-11410A>T